The synthesis of amides and dipeptides from unprotected amino acids by a simultaneous protection–activation strategy using boron trifluoride diethyl etherate-Reference-Cited by-同舟云学术

The synthesis of amides and dipeptides from unprotected amino acids by a simultaneous protection–activation strategy using boron trifluoride diethyl etherate

Published:2005-01 Issue:4 Volume:46 Page:653-656
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

van Leeuwen S.H.,Quaedflieg P.J.L.M.,Broxterman Q.B.,Milhajlovic Y.,Liskamp R.M.J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Peptidsynthesen in wäßriger Phase. Synthese einiger Peptide und eines Fehlsequenzpeptid-Gemisches mit derN-Carboxyanhydrid-Methode

2. Stepwise synthesis of oligopeptides with N-carboxy-.alpha.-amino acid anhydrides. IV. N-Carboxyglycine anhydride

3. Controlled synthesis of peptides in aqueous medium. VIII. Preparation and use of novel .alpha.-amino acid N-carboxyanhydrides

4. Facile synthesis of block copolypeptides of defined architecture

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2. Amidation of α-Amino Acids Using Dichloro(methyl)(3,3,3-trifluoropropyl)silane and Imidazole without Conventional Protection and Deprotection of α-Amino Group;Synlett;2022-05-31

3. Peptide bond formation using unprotected N-carboxyanhydrides under green chemistry conditions;Sustainable Chemistry and Pharmacy;2021-12

4. Peptide Bond Formation of Amino Acids by Transient Masking with Silylating Reagents;Journal of the American Chemical Society;2021-04-30

5. Peptide‐Chain Elongation Using Unprotected Amino Acids in a Micro‐Flow Reactor;Chemistry – A European Journal;2019-10-24